Pathways - manually collected, often from reviews:
OpenBEL Selventa BEL large corpus:
AIFM1
→
PARP1
(increases, PARP1 Translocation, AIFM1 Activity)
Xu et al., J Biol Chem 2006* Evidence: We found, based on genetic knockouts and pharmacological inhibition, that c-Jun N-terminal kinase (JNK), especially JNK1, but not the other groups of mitogen-activated protein kinase, is required for PARP-1-induced mitochondrial dysfunction, apoptosis-inducing factor translocation, and subsequent cell death.
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *